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. 2015 Nov 30;112(50):15354–15359. doi: 10.1073/pnas.1510944112

Table S1.

CDR sequence, affinity, and stability characteristics of parental, grafted, and ABS-derived lead clones

CDRL1* CDRL2 CDRL3 CDRH1 CDRH2 CDRH3 % germ line in CDRs No. of FW mutations IC50 (nM) HTRF kDa (nM) SPR % Agg 60 °C Tm (°C) % Loss in pH shock
DPK9/DP54 RASQSISSYLN AASSLQS QQSYSTPLT GFTFSSYWMS ANIKQDGSEKYYVDSVKG n/a 100 n/a n/a n/a n/a n/a n/a
CL-Hum-RAGE RASQDVGIYVN RATNLAD LEFDEHPLT GFTFSNYWMT ASIDNSGDNTYYPDSVKD GGDITTGFDY 45 5 10.3 31.0 14 77 4.8
Graft-RAGE RASQDVGIYVN RATNLAD LEFDEHPLT GFTFSNYWMT ASIDNSGDNTYYPDSVKD GGDITTGFDY 45 0 >61.9 ND 0 84 1.0
C7-ABS-RAGE RASQSIGSYLN RASSLAS LEFDEHPLT GFTFSSYWMS ASIDQDGSNKYYPDSVKG GGDITTGLDY 74 0 5.8 17.0 2 85 2.3
DPK9/DP47 RASQSISSYLN AASSLQS QQSYS–TPLT GFTFSSYAMS SAISGSGGSTYYADSVKG n/a 100 n/a n/a n/a n/a n/a n/a
Par-A33 LASEFLFNGVS GASNLES LGGYSGSSGLT GIDFSHYGIS AYIYPNYGSVDYASWVNG DRGYYSGSRGTRLDL 39 n/a 2.9 2.1 7 74 1.4
Graft-A33 LASEFLFNGVS GASNLES LGGYSGSSGLT GIDFSHYGIS SYIYPNYGSVDYASWVNG DRGYYSGSRGTRLDL 39 0 ND ND ND ND ND
C6-ABS-A33 RASQFLFNGVS AASNLES QGGYSGSTGLT GFTFSHYGIS SYIYPSYGSTDYASSVKG DRGYYSGSRGTRLDL 56 0 2.7 2.1 8 74 0.5
DPL16/DP47 QGDSLRSYYAS GKNNRPS NSRDSSGNHVV GFTFSSYAMS SAISGSGGSTYYADSVKG n/a 100 n/a n/a n/a n/a n/a n/a
Par-pTau SGSDYDYG- WNDKRPS GAYDGSAGGGI GFTLSSYQMM AGITSRGGVTGYGSAVKG PALDSDQCGFPEAGCIDA 41 n/a 1.6 0.41 17 70 1.2
Graft-ABS-pTau SGSDYDYG- WNDKRPS GAYDGSAGGGI GFTLSSYQMM AGITSRGGVTGYGSAVKG PALDSDQCGFPEAGCIDA 41 0 >64.7 NB 90 66 0.8
C21-ABS-pTau QGDD–SYYG- GNDNRPS GAYDSSGGGGI GFTLSSYQMM AGITGRGGVTGYADSVKG PALDSDQCGFPEAGCIDA 65 1 2.1 0.25 3 70 1.4
Com-ABS-pTau QGDD–SYYG- GNNNRPS GSYDSSGGHGV GFTFSSYQMS SGITGRGGVTGYADSVKG PALDSDQCGFPEMGCIDA 76 1 ND 0.50 2 71 0.8
*

The pTau CDR-L1 is shorter than its DPL16 counterpart by 3 amino acids. Sequence dashes in this CDR are added to show the spacing of sampled residues, based on sequence alignment. Residues differing from human germ line are underlined. CDR definitions used in this manuscript are an expanded definition in comparison with the classical Kabat, including VH positions 26–29 and 49.